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Clinical trial protocol for the evaluation of intraoperative near-infrared fluorescence imaging of pulmonary nodule by inhalation of indocyanine green

Clinical trial protocol for the evaluation of intraoperative near-infrared fluorescence imaging of pulmonary nodule by inhalation of indocyanine green

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100047326
Enrollment
Unknown
Registered
2021-06-12
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary nodule

Interventions

Sponsors

Key Laboratory of Molecular Imaging,Chinese Academy of Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years; 2. Size of pulmonary nodule: minor diameter <= 3.0cm; 3. Distance from pleura <= 1.0cm; 4. Type of pulmonary nodule: solid, ground glass.

Exclusion criteria

Exclusion criteria: 1. Indocyanine green allergies; 2. History of inhalation allergies; 3. History of chest surgery; 4. Asthma, pulmonary atelectasis, pleural adhesions or pulmonary dysfunction.

Design outcomes

Primary

MeasureTime frame
Pulmonary nodule detection rate;Positive margin rate;

Countries

China

Contacts

Public ContactWang Kun
kun.wang@ia.ac.cn+86 18612965656

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026